Evidence map›Paper›PMID 29154543›Full record

ArticleJournal of the American Chemical Society2017

Fluorogenic Targeting of Voltage-Sensitive Dyes to Neurons.

Pei Liu, Vincent Grenier, Wootack Hong, Vikram R Muller, Evan W Miller

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.8field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Article
  3. Fluorogenic rhodamine B derivatives that become brighter at neutral pH.Bioorganic & medicinal chemistry letters · 2026
    Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Voltage Imaging inFrontiers in neuroscience · 2021
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Pei LiuDepartment of Chemistry, ‡Department of Molecular and Cell Biology, and §Helen Wills Neuroscience Institute, University of California , Berkeley, California 94720, United States.
Vincent GrenierDepartment of Chemistry, ‡Department of Molecular and Cell Biology, and §Helen Wills Neuroscience Institute, University of California , Berkeley, California 94720, United States.
Wootack HongDepartment of Chemistry, ‡Department of Molecular and Cell Biology, and §Helen Wills Neuroscience Institute, University of California , Berkeley, California 94720, United States.
Vikram R MullerDepartment of Chemistry, ‡Department of Molecular and Cell Biology, and §Helen Wills Neuroscience Institute, University of California , Berkeley, California 94720, United States.
Evan W MillerDepartment of Chemistry, ‡Department of Molecular and Cell Biology, and §Helen Wills Neuroscience Institute, University of California , Berkeley, California 94720, United States.ORCID 0000-0002-6556-7679
University of California, Berkeley · US

Funding

Interrogating Neuronal Membrane Potential Dynamics with Optical Voltage SensorsR01NS098088 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI Evan Walker Miller · 2017 to 2026
$4.4M
New Chemical Tools for Exploring Cellular PhysiologyR35GM119855 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI MILLER, EVAN WALKER · 2016 to 2020
$1.3M
NIGMS NIH HHS R35 GM119855NINDS NIH HHS R01 NS098088
6 · The paper itself

Abstract

We present a method to target voltage-sensitive fluorescent dyes to specified cells using an enzyme-catalyzed fluorogenic reaction on cell surfaces. The dye/enzyme hybrids are composed of a photoinduced electron transfer (PeT)-based fluorescent voltage indicator and a complementary enzyme expressed on the cell surface. Action of the exogenous enzyme on the dye results in fluorogenic activation of the dye, enabling fast voltage imaging in defined neurons with sensitivity surpassing those of purely genetically encoded approaches. We employ a bulky methylcyclopropylacetoxymethyl ether to diminish the fluorescence of a PeT-based voltage-sensitive dye, or VoltageFluor. The hydrolytically stable ether can be removed by the action of porcine liver esterase (PLE) to reveal the bright unmodified VoltageFluor. We established that the chemically modified VoltageFluor is a substrate for PLE in vitro and in live cells. When PLE is targeted to the external face of cell membranes, it controls the apparent staining of cells. The use of neuron-specific promoters can direct staining to mammalian neurons to provide clear detection of neuronal action potentials in single trials. All of the new VoltageFluors targeted by esterase expression (VF-EXs) report single spikes in cultured mammalian neurons. The best, VF-EX2, does so with a signal-to-noise ratio nearly double that of comparable genetically encoded voltage reporters. By targeting PLE to neurons, VF-EX2 can interrogate the neuromodulatory effects of serotonin in cultured hippocampal neurons. Taken together, our results show that a combination of synthetic chemistry and biochemistry enables bright and fast voltage imaging from genetically defined neurons in culture.

Indexed as

Action PotentialsAnimalsCell MembraneFluorescent DyesHEK293 CellsHippocampusHumansNeuronsFluorescent Dyes

Identifiers

PMID29154543
PMCPMC5718920
OpenAlexW2769977504

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.